EWS rabbit pAb

EWS rabbit pAb

AO-06-ES2308-100

EWS rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES2308
Product nameEWS rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA
Other nameEWSR1; EWS; RNA-binding protein EWS; EWS oncogene; Ewing sarcoma breakpoint region 1 protein
Size100μL
Unit price ($)248
Human gene ID2130
Human Swiss-ProtQ01844
SourceRabbit
IsotypeIgG
TargetEWS
Fields>>Transcriptional misregulation in cancer
Gene nameEWSR1
Protein nameRNA-binding protein EWS
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID14030
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ61545
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenThe antiserum was produced against synthesized peptide derived from human EWSR1. AA range:403-452
SpecificityEWS Polyclonal Antibody detects endogenous levels of EWS protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/10000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)68kD
BackgroundThis gene encodes a multifunctional protein that is involved in various cellular processes, including gene expression, cell signaling, and RNA processing and transport. The protein includes an N-terminal transcriptional activation domain and a C-terminal RNA-binding domain. Chromosomal translocations between this gene and various genes encoding transcription factors result in the production of chimeric proteins that are involved in tumorigenesis. These chimeric proteins usually consist of the N-terminal transcriptional activation domain of this protein fused to the C-terminal DNA-binding domain of the transcription factor protein. Mutations in this gene, specifically a t(11;22)(q24;q12) translocation, are known to cause Ewing sarcoma as well as neuroectodermal and various other tumors. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been id
Functiondisease:A chromosomal aberration involving EWSR1 is associated with desmoplastic small round cell tumor (DSRCT). Translocation t(11;22)(p13;q12) with WT1.,disease:A chromosomal aberration involving EWSR1 is associated with malignant melanoma of soft parts (MMSP). Translocation t(12;22)(q13;q12) with ATF-1. Malignant melanoma of soft parts, also known as soft tissue clear cell sarcoma, is a rare tumor developing in tendons and aponeuroses.,disease:A chromosomal aberration involving EWSR1 is associated with small round cell sarcoma. Translocation t(11;22)(p36.1;q12) with PATZ1.,disease:Chromosomal aberrations involving EWSR1 are a cause of Ewing sarcoma [MIM:133450]. Translocation t(11;22)(q24;q12) with FLI1; translocation t(7;22)(p22;q12) with ETV1; translocation t(21;22)(q22;q12) with ERG; translocation t(9;22)(q22-31;q11-12) with NR4A3. Translocation t(2;21;22)(q23;q22;q12) that forms a
Subcellular locationNucleus . Cytoplasm . Cell membrane . Relocates from cytoplasm to ribosomes upon PTK2B/FAK2 activation.
ExpressionUbiquitous.

Additional Images

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Western Blot analysis of various cells using EWS Polyclonal Antibody
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Western Blot analysis of COLO205 cells using EWS Polyclonal Antibody
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Western blot analysis of the lysates from HepG2 cells using EWSR1 antibody.
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: AO-06-ES2308-100
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Hurry! only 10 items left in stock.

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